Transcriptional changes in the mammary gland during lactation revealed by single cell sequencing of cells from human milk
Alecia-Jane Twigger (),
Lisa K. Engelbrecht,
Karsten Bach,
Isabel Schultz-Pernice,
Sara Pensa,
Jack Stenning,
Stefania Petricca,
Christina H. Scheel () and
Walid T. Khaled ()
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Alecia-Jane Twigger: University of Cambridge
Lisa K. Engelbrecht: Helmholtz Zentrum München
Karsten Bach: University of Cambridge
Isabel Schultz-Pernice: Helmholtz Zentrum München
Sara Pensa: University of Cambridge
Jack Stenning: University of Cambridge
Stefania Petricca: Helmholtz Zentrum München
Christina H. Scheel: Helmholtz Zentrum München
Walid T. Khaled: University of Cambridge
Nature Communications, 2022, vol. 13, issue 1, 1-12
Abstract:
Abstract Under normal conditions, the most significant expansion and differentiation of the adult mammary gland occurs in response to systemic reproductive hormones during pregnancy and lactation to enable milk synthesis and secretion to sustain the offspring. However, human mammary tissue remodelling that takes place during pregnancy and lactation remains poorly understood due to the challenge of acquiring samples. We report here single-cell transcriptomic analysis of 110,744 viable breast cells isolated from human milk or non-lactating breast tissue, isolated from nine and seven donors, respectively. We found that human milk largely contains epithelial cells belonging to the luminal lineage and a repertoire of immune cells. Further transcriptomic analysis of the milk cells identified two distinct secretory cell types that shared similarities with luminal progenitors, but no populations comparable to hormone-responsive cells. Taken together, our data offers a reference map and a window into the cellular dynamics that occur during human lactation and may provide further insights on the interplay between pregnancy, lactation and breast cancer.
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27895-0
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DOI: 10.1038/s41467-021-27895-0
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